178.18 g/mol. Cinnamic acid is an organic compound with the formula C 6 H 5 CH=CHCOOH. It derives from a cinnamic acid. Learn more at http://www.doceri.com n D20 1.559-1.561. While working with material safety data sheets (MSDS), I found that manufacturers sometimes used obscure names for constituent chemicals and I didn't always have a good idea of what I was dealing with. Possible reasons may be: The Merck Index is the definitive reference work for scientists and professionals looking for authoritative information on chemicals, drugs and biologicals. Soluble in 3 vols of 70% alc. {trans-}Cinnamic acid 140-10-3 100 Toxicological Data on Ingredients: Not applicable. Articles of trans-Cinnamic acid are included as well. A series of cinnamic acid derivatives were synthesized and their biological abilities on lipoprotein metabolism were examined. Cinnamic acid, α-me thyl-MFCD00002652 [MDL number] α-Methylcinnamic ac id. The cinnamic acid is soluble in dichloromethane at room temperature and thus before the bromine addition the reaction vessel holds a colourless solution. Miscible with alcohol, ether. Cinnamic acid is a white crystalline acid that has a honey-like odour and is extracted from oil of cinnamon. This video screencast was created with Doceri on an iPad. hydroxyderivatives of cinnamic acid. mp 6-10°. Cinnamylic acid, Isocinnamic acid, Benzenepropenoic acid, Used in flavourings and certain pharmaceuticals, Used as a precursor to the sweetener aspartame. 2020-12-19. Calculate the number of mmol of Br2 present in 0.48 mL of bromine solution. Chemsrc provides trans-Cinnamic acid(CAS#:140-10-3) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Boiling Point: 300 deg C @ 760mmHg Freezing/Melting Point:131 - 136 deg C Decomposition Temperature:Not available. Doceri is free in the iTunes app store. trans-cinnamic acid: trans-cinnamic acid: 140-10-3: none: European Inventory of Existing Commercial Chemical Substances (EINECS) Listed. Your email address will not be published. Chemical Database Cinnamic Acid Identifications. FEMA Number 2288 . Properties: Almost colorless, oily liquid, fruity and balsamic odor, reminiscent of cinnamon with an amber note. It is collected from the oil of cinnamon and is also found in shea butter. The cinnamic acid is soluble in dichloromethane at room temperature and thus before the bromine addition the reaction vessel holds a colourless solution. Solubility: 0.4 g/l in water (20°C) Specific Gravity/Density:1.248 Molecular … Linear Formula C 6 H 5 CH=CHCOOH . Cinnamic acid, α-me thyl-MFCD00002652 [MDL number] α-Methylcinnamic ac id. It is found in Cinnamomum cassia. . General information; Classification & Labelling & PBT assessment; Manufacture, use & exposure EC number: 205-398-1 | CAS number: 140-10-3 . Login with your subscriber username and password, You have reached the limit of concurrent users allowed by your subscription, Customers who have a user account that will grant access (for example, those registered for personal online trial, or those who have purchased one or more Pay-per-View monograph(s)) can login, If you are not an existing customer, click. Cinnamic acids play key roles in the formation of other more complex phenolic compounds. GC-MS and HPLC analysis of these fractions resulted in the identification of several cinnamic acid derivatives, such as coumaric acid, caffeic acid and protocatechuic acid. Classified as an unsaturated carboxylic acid, it occurs naturally in a number of plants. This deamination relies on the MIO prosthetic group of PAL. The couples of compounds differed for the kind of aromatic substitution (p-hydroxy, p-hydroxymethoxy, p-hydroxydimethoxy, dihydroxy). trans-Cinnamic acid is an α,β-unsaturated aromatic acid that can be used as a flavoring agent. Vapor Density: Not available. Determine the melting points of pure samples of cinnamic acid and urea as well as a 50:50 mixture of the two, and record the data in your lab notebook. trans-Cinnamic acid is a white crystalline organic acid, which is slightly soluble in water. PubChem Substance ID 24893022. After the addition of bromine to trans-cinnamic acid, the product was identified by its melting point and infrared spectrum resulting in erythro-2,3-Dibromo-3-phenylpropanoic acid after comparing similar properties. At last,trans-Cinnamic acid… Skip to page content; Skip to site menu on this page. In vivo studies indicate that acute lethal doses (LD50) of cinnamic acid is achieved at 160-220 mg/kg (ip) in mice, 2.5 g/kg (oral) in rats and 5 g/kg (dermal) in rabbits. Section 3: Hazards Identification Potential Acute Health Effects: Slightly hazardous in case of skin contact (irritant), of eye contact (irritant), of ingestion, of inhalation. To prepare a 50:50 mixture, mix equal small portions of these compounds (estimate See more. The concentration causing a 50% reduction of cell proliferation (IC 50) ranged from 1 to 4.5 mM in glioblastoma, melanoma, prostate and lung carcinoma cells. What is the theoretical yield of the addition product? Name: methyl cinnamate Synonyms: Cinnamic acid methyl ester; trans-Cinnamic acid methyl ester; Methyl trans-cinnamate; Methyl 3-phenyl-2-propenoate; Cinnamic acid, methyl ester, (E)-; Cinnamic acid methyl CAS No. EC Inventory: Listed. It has a honey-like odour. The Merck Index* Online | Cinnamic Acid | Monograph containing literature references, physical and biological properties and relevant information It has a role as a plant metabolite. 2005-03-26. 4-methoxycinnamic acid is a methoxycinnamic acid having a single methoxy substituent at the 4-position on the phenyl ring. Create. The growth of four spoilage yeasts, Saccharomyces cerevisiae, Zygosaccharomyces bailii, Brettanomyces bruxellensis, and Brettanomyces naardenensis, was inhibited with three-agent (triplet) combinations of lauric arginate, cinnamic acid, and sodium benzoate or … We now show that cinnamic acid induces cytostasis and a reversal of malignant properties of human tumor cells in vitro. Chemsrc provides trans-Cinnamic acid(CAS#:140-10-3) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Insol in water. trans-Cinnamic acid Description These are organic aromatic compounds containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid. Doceri is free in the iTunes app store. (use a MW calculated to 2 decimal places) PAL catalyzes this reaction by a non-oxidative deamination. Bromination of Cinnamic acid Supplementary Material Experimental notes This experiment aims at the preparation of the 2,3-dibromo-3-phenylpropanoic acid from cinnamic acid by bromine addition. Articles of Cinnamic acid are included as well. Determination of L-phenylalanine. Display Name: trans-cinnamic acid EC Number: 205-398-1 EC Name: trans-cinnamic acid CAS Number: 140-10-3 Molecular formula: C9H8O2 IUPAC Name: (2E)-3-phenylprop-2-enoic acid Cinnamic acid is a monocarboxylic acid that consists of acrylic acid bearing a phenyl substituent at the 3-position. (use a MW calculated to 2 decimal places) PAL gives rise to trans-cinnamic acid. Abstract The bromination of trans-cinnamic acid was completed to determine dibromide’s stereochemical structure and its mechanism. Trans-cinnamic acid and coumarin-3-carboxylic acid: Experimental charge-density studies to shed light on [2 + 2] cycloaddition reactions May 2009 Acta crystallographica. PubChem Substance ID 24900955. Potential Chronic Health Effects: CARCINOGENIC EFFECTS: Not available. Calculate the number of mmol in 100. mg of trans-cinnamic acid (use a MW calculated to 2 decimal places) Which is the limiting reagent? However, in the case of . 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